NM_152536.4(FGD5):c.1611G>T (p.Leu537Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004348819.1
Allele description [Variation Report for NM_152536.4(FGD5):c.1611G>T (p.Leu537Phe)]
NM_152536.4(FGD5):c.1611G>T (p.Leu537Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens peptide deformylase-like protein mRNA, complete cds
Homo sapiens peptide deformylase-like protein mRNA, complete cdsgi|11320943|gb|AF239156.1|Nucleotide
-
box C/D snoRNA protein 1 isoform 2 [Homo sapiens]
box C/D snoRNA protein 1 isoform 2 [Homo sapiens]gi|282165825|ref|NP_001164141.1|Protein
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Last Updated: Oct 13, 2024